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Items: 1 to 20 of 141

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148201copy number variation1nstd102humanPathogenic GRCh38 chr3: 93,979,547-124,774,010 , GRCh37.p13 chr3: 93,698,391-124,492,857 NECTIN3, H2BP3, 418 more genes
    nsv7041333inversion1nstd229human GRCh38 chr3: 119,602,733-121,708,334 , GRCh37.p13 chr3: 119,321,580-121,427,181 RABL3, PTOV1P1, 44 more genes
    nsv7039920inversion1nstd229human GRCh38 chr3: 119,602,735-121,711,940 , GRCh37.p13 chr3: 119,321,582-121,430,787 LINC02049, GSK3B, 44 more genes
    nsv6707907copy number variation1nstd229human GRCh38 chr3: 113,856,250-122,791,940 , GRCh37.p13 chr3: 113,575,097-122,510,787 COX17, LOC105374052, 133 more genes
    nsv6705251copy number variation1nstd229human GRCh38 chr3: 119,617,774-119,678,934 , GRCh37.p13 chr3: 119,336,621-119,397,781 RPL10P7, POPDC2, 3 more genes
    nsv6704409copy number variation1nstd229human GRCh38 chr3: 119,468,099-119,806,079 , GRCh37.p13 chr3: 119,186,946-119,524,926 POPDC2, CFAP91, 13 more genes
    nsv6703931copy number variation1nstd229human GRCh38 chr3: 118,573,267-126,079,281 , GRCh37.p13 chr3: 118,292,114-125,798,124 RPS24P9, LOC105374064, 149 more genes
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6637150copy number variation1nstd102humanUncertain significance GRCh37 chr3: 116,109,191-120,328,013 , GRCh38.p12 chr3: 116,390,344-120,609,166 LOC101926953, LOC105374058, 60 more genes
    nsv6558695inversion1nstd223human GRCh38 chr3: 115,305,653-119,971,699 , GRCh37.p13 chr3: 115,024,500-119,690,546 LOC105374060, RN7SL815P, 52 more genes
    nsv6371858copy number variation1nstd223human GRCh38 chr3: 119,672,301-119,679,200 , GRCh37.p13 chr3: 119,391,148-119,398,047 COX17
    nsv6368772copy number variation1nstd223human GRCh38 chr3: 119,640,731-119,691,505 , GRCh37.p13 chr3: 119,359,578-119,410,352 POPDC2, COX17, 1 more genes
    nsv6357308copy number variation1nstd223human GRCh38 chr3: 119,617,774-119,678,928 , GRCh37.p13 chr3: 119,336,621-119,397,775 LOC105374063, PLA1A, 3 more genes
    nsv6313773copy number variation1nstd102humanUncertain significance GRCh37 chr3: 119,354,755-119,773,920 , GRCh38.p12 chr3: 119,635,908-120,055,073 NR1I2, LOC105374064, 8 more genes
    nsv6134575copy number variation1nstd213human GRCh37 chr3: 116,870,000-132,100,001 , GRCh38.p12 chr3: 117,151,153-132,381,157 ACP3, ADCY5, 308 more genes
    nsv5898228copy number variation1nstd209human GRCh38 chr3: 119,675,412-119,675,525 , GRCh37.p13 chr3: 119,394,259-119,394,372 COX17
    nsv5889494copy number variation1nstd209human GRCh38 chr3: 119,662,960-119,757,421 , GRCh37.p13 chr3: 119,381,807-119,476,268 LOC105374064, CFAP91, 2 more genes
    nsv5834859copy number variation1nstd209human GRCh38 chr3: 119,662,779-119,679,095 , GRCh37.p13 chr3: 119,381,626-119,397,942 LOC105374063, COX17
    nsv5092470mobile element insertion1nstd203human GRCh38 chr3: 119,676,371-119,676,383 , GRCh37.p13 chr3: 119,395,218-119,395,230 COX17
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
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